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Chemoattractant receptors as pharmacological targets for elimination of glioma stem-like cells

Journal

INTERNATIONAL IMMUNOPHARMACOLOGY
Volume 11, Issue 12, Pages 1961-1966

Publisher

ELSEVIER
DOI: 10.1016/j.intimp.2011.08.021

Keywords

Glioma; Cancer stem cells; Chemoattractant receptors; Chemokine receptors

Funding

  1. National Basic Research Program of China (973 Program) [2010CB529403]
  2. National Natural Science Foundation of China (NSFC) [30800421]
  3. Natural Science Foundation (CSTC) [2008BB5136]
  4. National Cancer Institute, National Institutes of Health [HHSN261200800001E]

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Malignant tumors are thought to be initiated by a small population of cells that display stem cell properties, including the capacity of self-renewal, multipotent differentiation, initiation of tumor tissues and resistance to therapy. Cancer stem cells (CSCs) have also been identified in gliomas in which they are named as glioma stem-like cells (GSLCs), or glioma stem cells. In xenograft transplantation models, GSLCs propagate tumor and promote tumor progression. The tumorigenesis of GSLCs depends not only on their autonomous proliferation but also on interaction with microenvironment components. Among these components, G protein coupled chemoattractant receptors (GPCRs) and their agonists have attracted much attention for their capacity to mediate leukocyte infiltration, angiogenesis, tumor invasion and metastasis. Chemoattractant GPCRs are widely expressed by tumor cells and stromal cells and recognize agonists present in the tumor microenvironment. Such GPCRs have been found to be expressed also by CSCs including GSLCs. In this brief review, we will summarize the recent development in the studies of the function, regulation and signal transduction of chemoattractant GPCRs in GSLCs in hope to promote a better understanding of the mechanistic basis of the progression of gliomas and the identification of molecular targets for the novel anti-glioma therapy. Published by Elsevier B.V.

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